Advanced oxidation of raw and biotreated textile industry wastewater with O-3, H2O2/UV-C and their sequential application

Citation
I. Arslan et Ia. Balcioglu, Advanced oxidation of raw and biotreated textile industry wastewater with O-3, H2O2/UV-C and their sequential application, J CHEM TECH, 76(1), 2001, pp. 53-60
Citations number
31
Categorie Soggetti
Biotecnology & Applied Microbiology","Chemical Engineering
Journal title
JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY
ISSN journal
02682575 → ACNP
Volume
76
Issue
1
Year of publication
2001
Pages
53 - 60
Database
ISI
SICI code
0268-2575(200101)76:1<53:AOORAB>2.0.ZU;2-8
Abstract
The advanced chemical oxidation of raw and biologically pretreated textile wastewater by (1) ozonation, (2) H2O2/UV-C oxidation and (3) sequential app lication of ozonation followed by H2O2/UV-C oxidation was investigated at t he natural pH values (8 and 11) of the textile effluents for 1 h. Analysis of the reduction in the pollution load was followed by total environmental parameters such as TOC, GOD, UV-VIS absorption kinetics and the biodegradab ility factor, f(B). The successive treatment combination, where a prelimina ry ozonation step was carried out prior to H2O2/UV-C oxidation without chan ging the total treatment time, enhanced the COD and TOC removal efficiency of the H2O2/UV-C oxidation by a factor of 13 and 4, respectively, for the r aw wastewater. In the case of biotreated textile effluent, a preliminary oz onation step increased COD removal of the H2O2/UV-C treatment system from 1 5% to 62%, and TOC removal from 0% to 34%. However, the sequential process did not appear to be more effective than applying a single ozonation step i n terms of TOC abatement rates. Enhancement of the biodegradability factor (fB) was more pronounced for the biologically pretreated wastewater with an almost two-fold increase for the optimized Advanced Oxidation Technologies (AOTs). For H2O2/UV-C oxidation of raw textile wastewater, apparent zero o rder COD removal rate constants (k(app)), and the second order OH. formatio n rates (r(i)) have been calculated. (C) 2001 Society of Chemical Industry.